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rs2278293

From SNPedia

Orientationminus
Stabilizedminus
Make rs2278293(A;A)
Make rs2278293(A;G)
Make rs2278293(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position128400698
GeneIMPDH1
is asnp
is mentioned by
dbSNPrs2278293
ebirs2278293
HLIrs2278293
Exacrs2278293
Varsomers2278293
Maprs2278293
PheGenIrs2278293
hapmaprs2278293
1000 genomesrs2278293
hgdprs2278293
ensemblrs2278293
gopubmedrs2278293
geneviewrs2278293
scholarrs2278293
googlers2278293
pharmgkbrs2278293
gwascentralrs2278293
openSNPrs2278293
23andMers2278293
23andMe allrs2278293
SNP Nexus

SNPshotrs2278293
SNPdbers2278293
MSV3drs2278293
GWAS Ctlgrs2278293
GMAF0.4444
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20679962OA-icon.png] Polymorphisms in type I and II inosine monophosphate dehydrogenase genes and association with clinical outcome in patients on mycophenolate mofetil


[PMID 20649757OA-icon.png] Inosine 5'-monophosphate dehydrogenase 1 haplotypes and association with mycophenolate mofetil gastrointestinal intolerance in pediatric heart transplant patients


[PMID 16384941OA-icon.png] Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.


[PMID 20061166] Genetic polymorphisms influence mycophenolate mofetil-related adverse events in pediatric heart transplant patients.


[PMID 20136638] Correlation of IMPDH1 gene polymorphisms with subclinical acute rejection and mycophenolic acid exposure parameters on day 28 after renal transplantation.


GET Evidence
rs2278293
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.460938
summary



[PMID 22960765] Inosine monophosphate dehydrogenase polymorphisms and renal allograft outcome.